US3681469A - Stabilization of 1,1,1-trichloroethane - Google Patents

Stabilization of 1,1,1-trichloroethane Download PDF

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US3681469A
US3681469A US74154A US3681469DA US3681469A US 3681469 A US3681469 A US 3681469A US 74154 A US74154 A US 74154A US 3681469D A US3681469D A US 3681469DA US 3681469 A US3681469 A US 3681469A
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trichloroethane
stabilization
reaction
aluminum
metals
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US74154A
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Wesley L Archer
Elbert L Simpson
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Dow Chemical Co
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Dow Chemical Co
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C17/00Preparation of halogenated hydrocarbons
    • C07C17/38Separation; Purification; Stabilisation; Use of additives
    • C07C17/42Use of additives, e.g. for stabilisation

Abstract

The reaction of 1,1,1-trichloroethane with metals in inhibited by the presence in the 1,1,1-trichloroethane of a small amount of benzyl fluoride and/or benzotrifluoride.

Description

United States Patent Archer et a1.
[451 Aug. 1, 1972 [54] STABILIZATION OF 1,1,1-
TRICHLOROETHANE [72] Inventors: Wesley L. Archer, Midland; Elbert L. Simpson, Auburn, both of Mich.
[73] Assignee: The Dow Chemical Company,
Midland, Mich.
[22] Filed: Sept. 21, 1970 [21] Appl. No.: 74,154
[52] US. Cl ..260/652.5 R, 252/162, 252/171 [51] Int. Cl. ..C07c 17/42, C070 17/40 [58] Field of Search ..260/652.5; 252/162, 171
[56] I References Cited UNITED STATES PATENTS 3,049,571 8/1962 Brown ..260/652.5
Primary Examiner-Howard T. Mars Att0rneyGriswold & .Burdick, J. Roger Lochhead and Glwynn R. Baker a 7] ABSTRACT The reaction of 1,1,1-trichloroethane with metals in inhibited by the presence in the 1,1,1-trichloroethane of a small amount of benzyl fluoride and/or benzotrifluoride.
1 Claim, No Drawings STABILIZATION OF 1 1 l -TRICHLOROETHANE BACKGROUND OF THE INVENTION This invention relates to the stabilization of chlorinated solvents. More particularly, the present invention concerns the stabilization of 1,1,1- trichloroethane in the presence of metals, such as aluminum, iron, brass, zinc and the like.
Chlorinated hydrocarbons such as trichloroethylene and perchloroethylene are commonly used as solvents in chemical processes, dry cleaning, and metal degreasing. Solvents of this type are subject to slow decomposition and oxidation reactions, particularly in the presence of impurities such as water, traces of acid or metal salts. Corrosion of metal surfaces in containers and process equipment and deterioration of solvent quality by formation of acidic and colored byproducts thereby become serious problems. Inhibitors such as acid scavengers and antioxidants are commonly added to these solvents in order to prevent such degradative reactions. Inhibitor concentrations are normally of the order of one percent by weight or less.
1,1,1-Trichloroethane poses a particularly difficult stabilization problem because of its unusual reactivity with the above metals, notably aluminum. Traces of metal salts, moisture or other impurities are not needed to initiate the 1,1,l-trichloroethane-aluminum reaction, for this reaction occurs spontaneously on a freshly exposed aluminum surface with spectacular results, converting the solvent and the metal surface in a few minutes to a blackened mass of acidic, carbonaceous material and aluminum salts. Conventional acid acceptor stabilizers cannot be depended upon to inhibit the aluminum-l,1,1-trichloroethane reaction and suitable inhibitors must be discovered by independent investigation. The search has yielded few effective compounds and these show little or no obvious pattern of structure. Typical 1,1,1-trichloroethane formulations contain about 5 percent by weight of inhibitor which is usually a combination of compounds to inhibit reaction of the solvent with a variety of metals.
SUMMARY OF THE INVENTION It has now been found that the 1,1,l-trichloroethane tion of metals and 1,1,1-trichloroethane need be used. Although any significant amount will provide some inhibition, preferably about 0.1 to 1.0 gram mole per liter of 1,1,1-trichloroethane is employed.
SPECIFIC EMBODIMENTS The above compounds were tested forinhibiting activity in elongated glass test tubes having an inside diameter of 0.8 cm. and 33 cm. in length. To each vertically disposed tube there was added 0.54 g. of essentially pure 16-32 mesh granular aluminum and a solution of the inhibitor in purified 1,1,1-trichloroethane to make atotal volume of test ixture of 5 The c1 se en s o the test tubes were t en immerse in an 011 at held at a temperature sufficient to maintain the 1,1,1- trichloroethane solution in each tube at a steady reflux. The results listed in the following examples indicate the minimum concentration of the inhibitor found effective to provide complete inhibition of the 1,1,1- trichloroethane-aluminum reaction for 24 hours under these conditions. Prevention of the reaction for this length of time under the described conditions indicates capacity for effective inhibition for an indefiniteperiod. Concentrations are given in gram moles per liter. this figure being convertible to weight percent by the equation (moles/liter) (mol. wt. of inhibitotl' Wt. percent 13.46 7
Effective Concentration Example Compound g.-moles/liter 1 benzyl fluoride 0.017 2 benzotrlfluorlde 0.50
Additional tests, utilizing 2 l inch X l inch X 1/l6 rosion ratings are represented by numbers 0-5, where 0 is no corrosion up to 5 which is heavy corrosion.
Condition of coupons 2024 A1 1100 Al Iron Brass Zinc Fluoro compound L.1. VJ. 11.1. v.1. 11.1 v.1 L.l v.1 11.1. yr. Color of [lnul soln.
Bcnzyl lluoridc l) U 0 0 0 0 0 1 .2 0 'lurbid but colorless. Benzotrilluoritle l) 0 t) 0 0 U 1 1 1 t) Colorless.
L.l. are liquid phase corrosion observations. -V.1. are vapor phase corrosion observations.
reaction can be substantially retarded or prevented by We claim:
incorporating into the 1,1,1-trichloroethane an inhibit ing amount of benzyl fluoride or benzotrifluoride. Such compounds may be used alone or in combination with each other or with other nonreactive conventional inhibitors, such as nitromethane and an epoxide.
Only a quantity of benzyl fluoride and/or benzotrifluoride sufficient to retard or to stop the reac- 1. A 1,1,1-Trichloroethane composition stabilized against reaction with metals consisting essentially of
US74154A 1970-09-21 1970-09-21 Stabilization of 1,1,1-trichloroethane Expired - Lifetime US3681469A (en)

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Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3049571A (en) * 1960-03-18 1962-08-14 Dow Chemical Co Stabilized degreasing solvent
US3360575A (en) * 1963-11-20 1967-12-26 Dow Chemical Co Stabilized solvent system
US3445532A (en) * 1962-10-18 1969-05-20 Dynamit Nobel Ag Stabilization of 1,1,1-trichloroethane
US3499047A (en) * 1958-02-03 1970-03-03 Ppg Industries Inc Stabilized compositions
US3505415A (en) * 1963-05-18 1970-04-07 Dynamit Nobel Ag Process for stabilizing 1,1,1-trichlorethane
US3564063A (en) * 1958-02-03 1971-02-16 Ppg Industries Inc Stabilized methylchloroform compositions
US3565811A (en) * 1967-12-29 1971-02-23 Dow Chemical Co Stabilized 1,1,1-trichloroethane composition

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3499047A (en) * 1958-02-03 1970-03-03 Ppg Industries Inc Stabilized compositions
US3564063A (en) * 1958-02-03 1971-02-16 Ppg Industries Inc Stabilized methylchloroform compositions
US3049571A (en) * 1960-03-18 1962-08-14 Dow Chemical Co Stabilized degreasing solvent
US3445532A (en) * 1962-10-18 1969-05-20 Dynamit Nobel Ag Stabilization of 1,1,1-trichloroethane
US3505415A (en) * 1963-05-18 1970-04-07 Dynamit Nobel Ag Process for stabilizing 1,1,1-trichlorethane
US3360575A (en) * 1963-11-20 1967-12-26 Dow Chemical Co Stabilized solvent system
US3565811A (en) * 1967-12-29 1971-02-23 Dow Chemical Co Stabilized 1,1,1-trichloroethane composition

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